+91-9666438880
indiaord@gmail.com
IORD – Indian Organization for Rare DiseasesIORD – Indian Organization for Rare DiseasesIORD – Indian Organization for Rare DiseasesIORD – Indian Organization for Rare Diseases
  • Home
  • About Us
    • Management Committee
    • Advisory Board
    • Newsletters
    • Newsletter Subscription
  • Rare Diseases
  • Research
  • Services
  • Donate
  • Gallery
    • Photo Gallery
      • World Rare Disease Day – 2023
      • World Rare Disease Day 2020
    • Video Gallery
      • World Rare Disease Day – 2020
      • World Rare Disease Day – 2019
      • World Rare Disease Day – 2018
  • Blog
  • Contact Us

US FDA approved Hemgenix to cost Rs 28.52 Crore!

    Home News US FDA approved Hemgenix to cost Rs 28.52 Crore!
    NextPrevious
    US FDA Approves World's Costliest Gene Therapy Drug for Hemophilia B

    US FDA approved Hemgenix to cost Rs 28.52 Crore!

    By IORD | News, Rare Disease News | 0 comment | 25 November, 2022 | 0

    The United States Federal Drug Administration (FDA) has approved a new gene therapy treatment for a rare blood clotting disease called Hemophilia B. The drug Hemgenix costs US$ 3.5mn (Rs 28.52 Crore). 

    Until now, the world’s costliest drug was Zolgensma – a drug for gene therapy used to treat children below two years diagnosed with ultra-rare genetic disease Spinal Muscular Atrophy (SMA) Type 1.

    However, with the US FDA approving the one-time gene therapy drug Hemgenix on November 22, 2022, it has now become the world’s heftiest-priced drug! The approval was granted to CSL Behring LLC, a global rare disease biotech company.

    The gene therapy drug is known to treat a rare genetic blood disorder called haemophilia B (Congenital Factor IX deficiency), which causes reduced clotting of the blood leading to excessive and uncontrollable bleeding.

    Taken intravenously, the US FDA in its approval letter says that the one-time drug HEMGENIX is an ‘adeno-associated virus vector-based gene therapy indicated for the treatment of adults with Hemophilia B.

    The US FDA website note says the drug can be used for Hemophilia B adult patients under the following conditions:

    • Those who currently use Factor IX prophylaxis therapy or
    • Have current or historical life-threatening haemorrhage, or
    • Have repeated, serious spontaneous bleeding episodes.

    The US FDA approved this drug after two successful clinical studies. “The safety and effectiveness of Hemgenix were evaluated in two studies of 57 adult men 18 to 75 years of age with severe or moderately severe Hemophilia B,” the US FDA notes on its website publication.

    Science Alert writes in this article that “Hemophilia B tends to be more common in men than women, and while an exact number is hard to come by, estimates suggest nearly 8,000 men in the US currently suffer from the lifelong disease.”

    It is also observed by Science Alert that the exorbitantly high cost of US$ 3.5mn (Rs 28.52 Crore) for Hemgenix is actually “reasonable” if the existing lifetime costs of Hemophilia B are taken into account. 

    “Today, researchers estimate the adult lifetime cost for every patient with moderate to severe haemophilia B is around US$21 to $23 million. Treatment costs in the UK are cheaper than in the US or elsewhere in Europe, but still add up to tens of millions of dollars per patient over their lifetime” says the article.

    No tags.

    IORD

    More posts by IORD

    Related Post

    • Genetics

      This Is An Era Of Genetics

      By IORD | 0 comment

      Prof. Ramaiah Muthyala delivering a talk on rare diseases in India, in Visakhapatnam on Monday. — PHOTO: C.V. SUBRAHMANYAM This is the era of genetics and not IT anymore, asserted a professor from University ofRead more

    • Rare and Ignored

      By IORD | 0 comment

      Rama was born normal. By the time she was six, her life underwent catastrophic events — blindness, breathing problems, asthma, growth problems. These resulted in consultations with multiple doctors and repeated hospitalization. After six years,Read more

    • RGI Refuses To Incorporate Patient Data In Census

      By IORD | 0 comment

      Citing space constraints in Census questionnaires and increase in workload of already-overworked enumerators with data related works, the Registrar General of India has turned down the proposal of the Indian Organisation for Rare Diseases (IORD),Read more

    • Policy For Rare Diseases On Anvil But Fails To Tap Into Patient Knowledge

      By IORD | 0 comment

      Hyderabad: While the Centre has made attempts to address the problem of rare diseases and even finalised a draft policy for rare diseases, experts say that the draft has completely missed out on covering theRead more

    • Centre Urged To Include Survey On Rare Diseases In Upcoming Census

      By IORD | 0 comment

      Hyderabad: Members of the Indian Organization of Rare Diseases (IORD), an umbrella organisation representing patients and patient groups of rare diseases have sent a proposal to the Centre that a questionnaire should be included inRead more

    • Centre Removes Data On Rare Diseases Prevalence Rate

      By IORD | 0 comment

      This has hit the patients who are suffering from rare diseases like thalassemia, sickle cell anaemia, lysosomal storage disorders, Hirschsprung’s disease, Gaucher’s disease, cystic fibrosis, haemangiomas and certain forms of muscular dystrophy. Those suffering fromRead more

    • Hyderabad Observes World Rare Disease Day

      By IORD | 0 comment

      World Rare Disease Day was observed on Friday, here at Hyderabad Millions of people around the world observe Rare Disease Day on the last day of February. “Some rare diseases, such as cystic fibrosis, thalassemia,Read more

    • Rare Disease Day

      IORD’s World Rare Disease Day-2020

      By IORD | 0 comment

      You are not alone as we all are one! Doctors, Survivors, Expert Speakers, Healthcare Staff, Patients’ Organizations, Rare Disease Patients, Researchers, Policy Makers, Rare Disease Volunteers, Parents and Students enthusiastically participated in IORD’s conference onRead more

    NextPrevious

    Categories

    • ANI
    • Deccan Chronicle
    • Economic Times
    • Eenadu
    • Events
    • IORD in News
    • IORD Updates
    • News
    • Pharmabiz.com
    • Rare Disease News
    • Telangana Today
    • The Hans India
    • The Hindu
    • The Pioneer
    • Times Now
    • Times of India
    • Uncategorised
    • Vaartha

    Recent Posts

    • My Battle with Porphyria: Why Jagruti Urges Nationwide Access to Hemin
    • May 2025: Rare Disease Updates, New Discoveries, Diagnostics, and Therapies
    • 78th WHA Takes Historic Step with Rare Diseases Resolution, 10-Year Global Plan Approved
    • India’s Rare Disease Crisis: Why Grassroots Solutions Are Urgently Needed
    • Advancing Rare Disease Awareness in India: Dr. Ramaiah Muthyala’s Strategic Insights

    Archives

    • June 2025
    • May 2025
    • April 2025
    • March 2025
    • February 2025
    • January 2025
    • December 2024
    • November 2024
    • September 2024
    • July 2024
    • June 2024
    • May 2024
    • March 2024
    • February 2024
    • December 2023
    • October 2023
    • July 2023
    • June 2023
    • May 2023
    • April 2023
    • March 2023
    • February 2023
    • January 2023
    • December 2022
    • November 2022
    • October 2022
    • September 2022
    • August 2022
    • June 2022
    • May 2022
    • April 2022
    • March 2022
    • February 2022
    • January 2022
    • December 2021
    • November 2021
    • October 2021
    • September 2021
    • July 2021
    • May 2021
    • April 2021
    • November 2020
    • March 2020
    • February 2020
    • January 2020
    • February 2019
    • January 2018
    • September 2015

    Follow Us

    IORD

    Indian Organization For Rare Diseases (IORD), a not-for-profit umbrella organization represents interests of all stakeholders of Rare Diseases in India including individual patients, patient support groups, health policy advocates and health care providers.

    RARE DISEASES

    • Rare Blood Diseases
    • Rare Heart Diseases
    • Rare Fungal Diseases
    • Rare Kidney Diseases
    • Rare Newborn Diseases
    • more...

    SERVICES

    • Research
    • Let's Come Together
    • Partner With Us
    • Volunteers
    • Privacy Policy
    • Sitemap

    CONTACT US

    Indian Organization For Rare Diseases
    Reg. Office (India): Plot 397, Road 22b, Jubilee Hills, Hyderabad (Telangana) 500033, Telangana, India

    Phone: +91-9666438880

    Email: indiaord@gmail.com

    © 2020 Indian Organization For Rare Diseases | All Rights Reserved. Powered By Digital Dynamics
    • Home
    • About Us
      • Management Committee
      • Advisory Board
      • Newsletters
      • Newsletter Subscription
    • Rare Diseases
    • Research
    • Services
    • Donate
    • Gallery
      • Photo Gallery
        • World Rare Disease Day – 2023
        • World Rare Disease Day 2020
      • Video Gallery
        • World Rare Disease Day – 2020
        • World Rare Disease Day – 2019
        • World Rare Disease Day – 2018
    • Blog
    • Contact Us
    IORD – Indian Organization for Rare Diseases